7p1m

Galectin-8 N-terminal carbohydrate recognition domain in complex with benzimidazole D-galactal ligand

Method: X-RAY DIFFRACTION Dmax: 73.6 Å Quality: GOOD

1. Protein Identity and Related Structures Protein Identity & Related Structures

Galectin-8

Homo sapiens

UniProt O00214

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 6–156 Chain B; UniProt 6–156 Not recorded 4IU 2-[[(2R,3R,4R)-2-(hydroxymethyl)-3-oxidanyl-3,4-dihydro-2H-pyran-4-yl]oxymethyl]-3-methyl-benzimidazole-5-carboxylic acid × 2 CL CHLORIDE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:LIQUID DIFFUSION;pH 8;293.5 K;Buffer (10mM Tris/HCl pH 8.0, 150 mM NaCl, 10 mm lactose and 1 mM TCEP) mixed with reservoir 25% (w/v) PEG 2000 monomethylethyer (MME), a cryo solution (10 mM Tris/HCl pH 8.0, 50 mM NaCl, 10 mM lactose, 25% (w/v) PEG 2000 MME, 20% ethylene glycol (EG) and 1 mM TCEP) and flash-frozen in liquid nitrogen. A co-crystal with lactose, grown from a seeded drop with 24% (w/v) PEG 2000 MME in the reservoir, was used to soak in compound 1 by transferring crystals in three steps to different soaking drops. First to a 2 ul drop with glycerol ( 20% (v/v) glycerol, 25% (w/v PEG 2000 MME, 10 mM Tris/HCl pH 8.0, 50 mM NaCl and 1 mM TCEP) and secondly to a 2 ul drop with 10 mM compound 1 (10 mM Tris/HCl pH 8.0, 50 mM NaCl, 5 mM compound 1, 25% (w/v) PEG 2000 MME and 1 mM TCEP) and thirdly to a second drop with 5 mM compound 1 (same composition as before). Resolution 1.52 Å R-free 0.207

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

36 other PDB entries and 55 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name LEG8_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–151; UniProt 6–156 Author chain B; PDBConstruct 1–151; UniProt 6–156

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 7p1m

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7p1m
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7p1m
Deposition date deposition_date2021-07-02
Structure title titleGalectin-8 N-terminal carbohydrate recognition domain in complex with benzimidazole D-galactal ligand
Keywords keywordsInhibitor, complex, Galectin, Lectin, D-galactal, Sugar binding protein; SUGAR BINDING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier22.67
Radius of gyration Rg (electron density) rg_electron21.82
Forward intensity I(0) i019536900.00
Molecular weight molecular_weight34476.0 kDa
Excluded volume excluded_volume43530 ų
Envelope volume envelope_volume51256 ų
Hydration-shell volume shell_volume20281 ų
Envelope diameter envelope_diameter76.2
Shell Rg shell_rg27.56
Envelope Rg envelope_rg22.00
Shape Rg shape_rg21.81
Total Rg total_rg22.62
Total atoms total_atoms2435
Residues n_residues299
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax73.6
Rg (real space) rg_real22.72
Rg uncertainty (real space) rg_real_error0.50
I(0) (real space) i0_real1.9540e+07
I(0) uncertainty (real space) i0_real_error2.7060e+05
Rg (reciprocal space) rg_reciprocal22.71
I(0) (reciprocal space) i0_reciprocal19540000.0000
Solution quality estimate total_estimate0.8853
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.4
Skewness Skewness skewness0.408
Kurtosis Kurtosis kurtosis-0.420
Angular range angular_range— – 0.3500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4206000.0000
Real-space data points n_real_points67
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.851; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.977; Smooth: 0.973

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)